This review highlights key aspects of the Tethered Aminohydroxylation from its discovery to its current incarnation, which employs N,O-acylated derivatives as reoxidants for osmium. The potential and generality of this reaction has been demonstrated by its application in the synthesis of several natural products. A review of the recently developed N-O reoxidants for the tethered aminohydroxylation (TA) reaction is presented. All aspects of the aminohydroxylation reactions that are facilitated are discussed, together with their application in total synthesis. Copyright © 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim
The aminohydroxylation reaction of olefins is a key organic transformation reaction, typically carri...
ABSTRACT: An iron-catalyzed diastereoselective inter-molecular olefin amino-oxygenation reaction is ...
The following account describes our work on the development and utilisation of the directed dihydrox...
This review highlights key aspects of the Tethered Aminohydroxylation from its discovery to its curr...
The first examples of amide-tethered aminohydroxylation reactions, catalyzed by osmium, showing that...
[reaction: see text] Changing the identity of the N leaving group on a hydroxylamine-based reoxidant...
The use of N-sulfonyloxy carbamates as reoxidants for the tethered aminohydroxylation (TA) reaction ...
The osmium-mediated aminohydroxylation reaction is a powerful oxidation that introduces a hydroxyl g...
In situ generated osmium-diamine chelates from 2,3-diaminopropionic acid or diaminosuccinic acid rep...
The oxidation of olefins is of central importance in organic synthesis. This thesis is divided into ...
The tethered aminohydroxylation of cyclic allylic carbamates is described using catalytic amounts of...
The utility of the tethered aminohydroxylation (TA) has been demonstrated by synthesis of the comple...
The cis dihydroxylation of alkenes is most efficiently accomplished by reaction with osmium tetroxid...
Since Sharpless' discovery of the asymmetric aminohydroxylation (AA) reaction, a major challenge for...
The osmium-catalyzed aminohydroxylation of glycals has been achieved with complete regio- and stereo...
The aminohydroxylation reaction of olefins is a key organic transformation reaction, typically carri...
ABSTRACT: An iron-catalyzed diastereoselective inter-molecular olefin amino-oxygenation reaction is ...
The following account describes our work on the development and utilisation of the directed dihydrox...
This review highlights key aspects of the Tethered Aminohydroxylation from its discovery to its curr...
The first examples of amide-tethered aminohydroxylation reactions, catalyzed by osmium, showing that...
[reaction: see text] Changing the identity of the N leaving group on a hydroxylamine-based reoxidant...
The use of N-sulfonyloxy carbamates as reoxidants for the tethered aminohydroxylation (TA) reaction ...
The osmium-mediated aminohydroxylation reaction is a powerful oxidation that introduces a hydroxyl g...
In situ generated osmium-diamine chelates from 2,3-diaminopropionic acid or diaminosuccinic acid rep...
The oxidation of olefins is of central importance in organic synthesis. This thesis is divided into ...
The tethered aminohydroxylation of cyclic allylic carbamates is described using catalytic amounts of...
The utility of the tethered aminohydroxylation (TA) has been demonstrated by synthesis of the comple...
The cis dihydroxylation of alkenes is most efficiently accomplished by reaction with osmium tetroxid...
Since Sharpless' discovery of the asymmetric aminohydroxylation (AA) reaction, a major challenge for...
The osmium-catalyzed aminohydroxylation of glycals has been achieved with complete regio- and stereo...
The aminohydroxylation reaction of olefins is a key organic transformation reaction, typically carri...
ABSTRACT: An iron-catalyzed diastereoselective inter-molecular olefin amino-oxygenation reaction is ...
The following account describes our work on the development and utilisation of the directed dihydrox...